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Division of Endocrinology and Metabolism, Departments of Medicine and Laboratory Medicine and Pathology (M. W.), University of Minnesota Minneapolis, Minnesota 55455
Address all correspondence and requests for reprints to: Cary N. Mariash, M.D., Box 91, Mayo Memorial Hospital, University of Minnesota, Minneapolis, Minnesota 55455.
We report a patient with pituitary-dependent Cushings syndrome in whom standard biochemical testing procedures failed to define the pituitary as the source of autonomous hormone secretion. Anomalous findings included: 1) wide variations of urinary steroid excretion during a 4-day dexamethasone suppression test, 2) a rise of the serum cortisol after the single dose (8 mg) overnight dexamethasone suppression test, 3) a diminished serum 11-deoxycortisol response to the metyrapone test, and 4) an absent plasma ACTH response to CRH. While the results of these studies were most consistent with an ectopic source of ACTH production, magnetic resonance imaging suggested that Cushings syndrome was due to a pituitary adenoma. The adenoma was removed by transphenoidal surgery. However, serum and urinary steroid levels remained measurable for 2 weeks because of the perioperative use of im cortisone acetate. Subsequent im administration of 200 mg cortisone acetate again led to prolonged serum and urinary steroid responses to this compound, thus emphasizing the pitfalls that may accompany the perioperative use of cortisone acetate. This patient demonstrates the importance of performing multiple tests, including magnetic resonance image scanning, in evaluation Cushings syndrome, since standard biochemical testing may not indicate pituitary ACTH hypersecretion as the cause.
* This work was supported by NIH Grants AM-19182 (to J.H.O.), DK-32885 (to C.N.M.), and Training Grant AM-07203.
Received March 21, 1988.
This article has been cited by other articles:
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T. B. Kaye and L. Crapo The Cushing Syndrome: An Update on Diagnostic Tests Ann Intern Med, March 15, 1990; 112(6): 434 - 444. [Abstract] [PDF] |
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